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Kristian Sneskov

Researcher at Aarhus University

Publications -  11
Citations -  1860

Kristian Sneskov is an academic researcher from Aarhus University. The author has contributed to research in topics: Coupled cluster & Excited state. The author has an hindex of 10, co-authored 11 publications receiving 1620 citations. Previous affiliations of Kristian Sneskov include University of Southern Denmark & Foundation Center.

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The Dalton quantum chemistry program system

Kestutis Aidas, +83 more
TL;DR: Dalton is a powerful general‐purpose program system for the study of molecular electronic structure at the Hartree–Fock, Kohn–Sham, multiconfigurational self‐consistent‐field, Møller–Plesset, configuration‐interaction, and coupled‐cluster levels of theory.
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Excited state coupled cluster methods

TL;DR: In this article, a review of coupled cluster (CC) theory for electronic excited states is presented, and the basics of a CC response theory framework that allows the transfer of the attractive accuracy and convergence properties associated with CC methods over to the calculation of electronic excitation energies and properties.
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The polarizable embedding coupled cluster method.

TL;DR: A new combined quantum mechanics/molecular mechanics (QM/MM) method based on a self-consistent polarizable embedding (PE) scheme is formulated and the relative importance of multipoles and polarizabilities in the description of two-photon absorption activity for formamide in aqueous solution is investigated.
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Scrutinizing the effects of polarization in QM/MM excited state calculations

TL;DR: A systematic investigation of solvent polarization effects by identifying lower order polarization reaction fields as compared to the full treatment, which constitutes an important step towards dissecting the accuracy of such calculations.
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Solvation Effects on Electronic Transitions: Exploring the Performance of Advanced Solvent Potentials in Polarizable Embedding Calculations.

TL;DR: It is illustrated that the use of advanced solvent potentials can provide higher accuracy compared to various simpler approaches for the prediction of solvent shifts and do so in a computationally competitive manner.